US3882940A - Tertiary oil recovery process involving multiple cycles of gas-water injection after surfactant flood - Google Patents
Tertiary oil recovery process involving multiple cycles of gas-water injection after surfactant flood Download PDFInfo
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- US3882940A US3882940A US425593A US42559373A US3882940A US 3882940 A US3882940 A US 3882940A US 425593 A US425593 A US 425593A US 42559373 A US42559373 A US 42559373A US 3882940 A US3882940 A US 3882940A
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 76
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 72
- 238000011084 recovery Methods 0.000 title claims abstract description 53
- 238000002347 injection Methods 0.000 title claims description 45
- 239000007924 injection Substances 0.000 title claims description 45
- 239000007789 gas Substances 0.000 claims abstract description 72
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 48
- 241000237858 Gastropoda Species 0.000 claims abstract description 27
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 22
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 22
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003345 natural gas Substances 0.000 claims abstract description 12
- 239000003570 air Substances 0.000 claims abstract description 11
- 239000001569 carbon dioxide Substances 0.000 claims abstract description 11
- 229910002092 carbon dioxide Inorganic materials 0.000 claims abstract description 11
- 239000003915 liquefied petroleum gas Substances 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 11
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 11
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000001294 propane Substances 0.000 claims abstract description 9
- 239000001273 butane Substances 0.000 claims abstract description 8
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims abstract description 8
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims abstract description 8
- 230000015572 biosynthetic process Effects 0.000 claims description 72
- 239000003208 petroleum Substances 0.000 claims description 58
- 238000000034 method Methods 0.000 claims description 42
- 239000012530 fluid Substances 0.000 claims description 36
- 239000000243 solution Substances 0.000 claims description 30
- 239000011148 porous material Substances 0.000 claims description 26
- 238000004519 manufacturing process Methods 0.000 claims description 15
- -1 ethylene, propylene, butylene Chemical group 0.000 claims description 12
- 238000004891 communication Methods 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 6
- 239000003546 flue gas Substances 0.000 claims description 6
- 230000006872 improvement Effects 0.000 claims description 6
- 239000003921 oil Substances 0.000 description 67
- 238000005755 formation reaction Methods 0.000 description 54
- 239000000463 material Substances 0.000 description 17
- 239000000126 substance Substances 0.000 description 16
- 230000008569 process Effects 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 9
- 238000006073 displacement reaction Methods 0.000 description 7
- 239000002736 nonionic surfactant Substances 0.000 description 7
- 230000000153 supplemental effect Effects 0.000 description 7
- 239000003945 anionic surfactant Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 229920001477 hydrophilic polymer Polymers 0.000 description 6
- 230000008901 benefit Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000008398 formation water Substances 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
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- 150000003871 sulfonates Chemical class 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 238000002955 isolation Methods 0.000 description 3
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- 238000004391 petroleum recovery Methods 0.000 description 2
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- 238000003307 slaughter Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- YCANCZRRZBHLEN-UHFFFAOYSA-N [N].O Chemical compound [N].O YCANCZRRZBHLEN-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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- 125000004430 oxygen atom Chemical group O* 0.000 description 1
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- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 235000019830 sodium polyphosphate Nutrition 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
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- 238000013517 stratification Methods 0.000 description 1
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- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Images
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
- E21B43/164—Injecting CO2 or carbonated water
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
Definitions
- This invention pertains to an oil recovery process and more particularly to a process for tertiary oil recovery. Still more particularly this invention is concerned with a method of treating an oil containing formation after the formation has been subjected to chemical tertiary I oil recovery treatment such as surfactant flooding so as r permitting the petroleum to flow to the surface through these wells. Recovery of petroleum from petroleum containing formations is possible only if certain conditions are satisfied.
- Water flooding which involves the injection of water into the subterranean,petroliferous formation for the purpose of displacing petroleum toward the producing well, is the most economical and most widely practiced supplemental recovery method.
- Water does not displace petroleum with high efficiency, however, since water and oil are immiscible, and also because the interfacial tension between water and oil is quite high.
- Persons skilled in the art of oil recovery have recognized this weakness of waterflooding and many additives have been described in the prior art for decreasing the interfacial tension between the injected water and the formation petroleum.
- This invention pertains to a novel process to be applied to a subterranean, petroleum containing formation which normally will already have been subjected to primary recovery and possibly waterflooding.
- the process is an additional step to be performed after subjecting the formation to chemical tertiary or supplemental oil recovery process such as flooding with a surfactant solution or a micellar dispersion.
- chemical tertiary or supplemental oil recovery process such as flooding with a surfactant solution or a micellar dispersion.
- each gas slug being from 1/10 to 10 pore volume percent and preferably from 2 to 8 pore volume percent in size, with water slugs of from 10 to 50 pore volume percent interposed therebetween, are used after the chemical flood.
- Gaseous materials suitable for use in this process include air, nitrogen, carbon dioxide, flue gas, exhaust gas, methane, ethane, propane, butane, natural gas, liquefied petroleum gas (LPG) and mixtures thereofjMy invention, therefor, comprises the process of using small, alternating gas and water slugs after a chemical flood such as an aqueous surfactant containing fluid.
- FIGURE illustrates the graphical results of a typical laboratory core displacement test, showing the pressure differential, percent oil recovery, residual oil saturation and water-oil ratio for a conventional waterflood followed by a surfactant flood followed by water injection followed by four cycles of gaswater injection.
- the process of my invention concerns an improvement in surfactant flooding.
- Surfactant flooding has been recognized by persons skilled in the art as a means for obtaining additional oil from an oil containing formation beyond that recoverable by primary recovery and waterflooding.
- the following explanation of surfactants and surfactant flooding provides a basis for understanding the prior art process with which my invention is to be used.
- the compound must be at least slightly soluble in at least one phase of the liquid system in which it is to be used.
- the compound must have an amphipathic structure (the molecule is composed of groups with opposing solubility tendencies). For use in oil recovery operations, the molecule must have at least one hydrophobic or oil soluble group and at least one hydrophilic or water soluble group.
- Surfactant molecules or ions tend to form oriented monolayers at phase interfaces.
- the equilibrium concentration of the surfactant in any particular solute is greater at the phase interface than the concentration of the surfactant in the bulk of the solution.
- the materials tend to form micelles or aggregates of molecules or ions whenever the concentration exceeds a certain limiting value which is a characteristic of the particular surfactant and solute.
- the material must exhibit some combination of the following functional properties: detergency, foaming, wetting, emulsifying, solubilizing and dispersing.
- Surfactants are generally classified in the literature on the basis of the type of hydrophilic or water soluble group or groups attached to the molecule, generally being classified as anionic, cationic or nonionic, as described below more fully.
- Anionic surfactants are those surfactant materials wherein the hydrophilic or water soluble group is a carboxylate, sulfonate, sulfate or phosphate group. This is the most important class of surfactants generally and as applied to oil recovery. Anionic surfactants are readily available, inexpensive, and have a high degree of surface activity. Petroleum recovery operations will generally involve the use of anionic surfactants unless there is some objection to the use of anionic surfactants, or some sufficient reason to resort to the use of some other compound. Petroleum sulfonates are currently very popular anionic surfactants for oil recovery, and are prepared by isolating a preselected boiling range fraction of a crude oil and subjecting it to sulfonation.
- Petroleum sulfonates are desirable for use in oil recovcry because of their effectiveness and low unit cost. Petroleum sulfonates do have certain limitations, however, notably their ineffectiveness in formations containing saline (high salt containing) or hard water (water having dissolved therein excessive quantities of polyvalent ions such as calcium and/or magnesium).
- Cationic surfactants employ primary, secondary, or tertiary amines, or quaternary ammonium groups, as the hydrophilic or water soluble group.
- Nonionic surfactants are materials which have no charge when the material is dissolved in an aqueous medium.
- the hydrophilic tendency is derived from oxygen atoms in the molecule which hydrate by hydrogen bonding to water molecules present in the solute.
- the strongest hydrophilic moiety in this class of surfactants is the ether linkage, and there must be a plurality of these linkages to render the compounds sufficiently water soluble to permit the compound to exhibit surface activity.
- Polyoxyethylene surfactants having the following recurring ether linkages are examples of hydrophilic moieties for nonionic surfactants:
- a nonionic surfactant molecule may have more than one chain containing ether linkages and generally as much as 60 to percent by weight of the molecule must be in the form of ether linkage containing chains in order to render the molecule sufficiently water soluble for it to function as a surfactant. It can be readily seen that the presence of these large chains containing the ether linkages in addition to the relatively long aliphatic or other hydrophobic chains results in a high molecular weight compound. and this is one reason that nonionic surfactants have low surface activity per unit weight of material. Nonionic surfactants are seldom used alone in oil recovery applications, although they are frequently employed in combination with another surfactant material, generally an anionic material.
- a preflush may be used to remove or displace water soluble materials present in the formation water which interfere with the surfactant material to be used.
- Sacrificial compounds such as sodium carbonate, sodium polyphosphate, sodium fluoride, etc., may also be present in the preflush to saturate the adsorption sites of the formation rock so as to minimize adsorption thereon of the subsequently injected surfactant. This slug may be followed by an isolation slug of water.
- the main displacing fluid is injected next, which may be an aqueous solution of one or several surfactants capable of reducing the interfacial tension between the formation petroleum and the injected aqueous fluids.
- the displacing fluid may also be an emulsion of a hydrocarbon in an aqueous surfactant solution.
- a mobility buffer fluid is generally introduced into the formation subsequent to the surfactant solution to displace the solution efficiently.
- a small isolation slug of water is sometimes used between the surfactant solution and the mobility buffer fluid.
- the mobility buffer fluid is needed to ensure efficient displacement of surfactant solution and formation petroleum which has been displaced by the surfactant solution because the mobility of the petroleum is less than the mobility of water.
- a dilute aqueous solution of a hydrophilic polymer such as polyacrylamide or a polysaccharide is used for this purpose.
- the concentration of polymer may be reduced gradually with time, or tapered, to essentially pure field water.
- percent oil recovery may often be increased by 10 to 20 percentage points, i.e., typically from 45 to 65 percent recovery, which may amount to millions of barrels of oil in a large field.
- percentage points i.e., typically from 45 to 65 percent recovery
- the cost of the materials is frequently so great that such a program is not economically viable even though it is technically successful.
- the additional treatment involves the injection of a plurality of small discrete slugs of a gaseous material separated by injecting small slugs of liquid, preferably water or other aqueous fluids.
- the volume of gas in each slug can be from 0.20 to 20 pore volume percent and usually the optimum size is from 2 to pore volume percent.
- the size of the water slug interposed between each gas slug injected can be from about 5 to about 50 pore volume percent, and preferably from about 10 to about pore volume percent.
- the number of discrete gas slugs injected can be from about 1 to about 20 and is preferably from about-2 to about 8 slugs.
- Air, nitrogen, carbon dioxide, normally gaseous paraffinic hydrocarbons such as methane, ethane, propane or butane as well as normally gaseous olefinic hydrocarbons such as ethylene, propylene or butylene and mixtures thereof are preferred gases for use in my invention.
- Crude gases such as exhaust gas or flue gas, which are predominantly carbon dioxide and nitrogen, as well as natural gas or liquefied petroleum gas (LPG) may also be used with excellent results.
- LPG liquefied petroleum gas
- gases are somewhat soluble in petroleum.
- carbon dioxide and the paraffinic hydrocarbons such as methane, ethane, etc., or the olefinic gases are quite soluble to varying degrees in petroleum. This is beneficial to the operation of my process since dissolution of these gases results in reduction in the viscosity of the petroleum; however, the solubility must be taken into consideration when determining the gas slug size.
- the solubility must be taken into consideration when determining the gas slug size.
- the gas and water may be injected simultaneously after completion of injection of the surfactant solution into the formation.
- the volume ratio of gas and water being injected should be from about 0.002 to about 1.5 and preferably from about 0.5 to about 1.0.
- Some precaution should be taken to avoid excess vertical stratification of the gas and water, gas going exclusively into the top portion of the formation and water moving exclusively into the bottom portion, because of the large differences in density between water and gas.
- density related vertical separation can be prevented, for example, by providing two separate injection strings and injecting gas into the bottom of the formation and water into the top of the formation. This arrangement also permits separate control of the injection rate of each material to maintain the desired ratio of gas and water.
- a subterranean, petroleum containing formation is found at a depth of 8000 feet.
- the formation is 40 feet thick and the porosity is 30 percent.
- the field is exploited first by primary production, utilizing a square grid pattern with 400 foot linespacing between wells.
- primary production which recovers only 25 percent of the original petroleum in place within the reservoir, injection wells are drilled in the center of each square grid to convert the field to an inverted five spot pattern for water injection.
- a large field entails a multiplicity of the square grid patterns, each 400 feet on a side and with an injection well in the center, it is possible to analyze the entire field by considering only a single grid unit.
- Water is injected into the injection well and production of oil is continued from the production wells until the water/oil ratio reaches 30, which is considered to be the economic limit for continued production.
- the water/oil ratio reaches 30, which is considered to be the economic limit for continued production.
- the formation water contains about 300 parts per million total hardness and low salinity, and tests indicate that petroleum sulfonate will function effectively therein.
- a tertiary chemical supplemental recovery program is designed using a 10 pore volume percent preflush comprising a 5 percent aqueous solution of sodium carbonate as a sacrificial adsorption agent followed by a 3 pore volume percent water slug to act as an isolation slug between the preflush and the surfactant slug.
- a 10 pore volume percent slug of 3.5 percent petroleum sulfonate is used as the surfactant slug. Since the pattern used results in percent sweep efficiency, the total pore volume swept by injected fluids in each grid segment is: 400 Ft. X 400 Ft.
- X 40 Ft. X 0.30 X 0.70 1,344,000 Cu. Ft..A percent pore volume slug of surfactant solution which amounts to 134,400 cu. ft. or 1,047,000 gallons, is used.
- the 1,047,000 gallons of 3.5 percent petroleum sulfonate surfactant solution is followed by injecting 1,000,000 gallons of an aqueous solution comprising 200 parts per million of polyacrylamide, a hydrophilic polymer in water, the solution having a viscosity of 8 centipoise. Finally, a pore volume percent slug of water is injected, followed by five cycles of alternating gas-water injection.
- Each cycle consists of injecting a 5 pore volume percent slug of natural gas which is 95 percent methane and the balance ethane and propane. Ten pore volume percent slugs of water follow each 5 pore volume percent slug of natural gas.
- continuous water injection is begun to displace all of the injected fluids through the formation and continued until the water-oil ratio of all of the wells has risen to a value above about 35.
- the average residual oil saturation is only 6 percent.
- Run D a core was subjected to a commercial waterflood employing a preflush with salinity optimization and containing sacrificial adsorption agents followed by an aqueous solution of petroleum sulfonate followed by an aqueous solution of a hydrophilic polymer for mobility control followed by waterflooding to a high water-oil ratio. A slug of nitrogen was then introduced and the core was again waterflooded.
- Run E was'performed as before exceptusing'two different commerciallyavailable surfactants-Ihesurfactant solution contained 1.0 percent Triton, a dioctyl sodium succinate and 0.25 percent TD-l5, a polyoxyalkalene ether.
- the results of Run E are given in Table IV below.
- Run F Two additional runs were made to compare a commercial chemical tertiary flood, Run F, comprising sacrificial agent preflush, petroleum sulfonate, hydrophilic polymer and waterflood to a high water-oil ratio, to a Run G which is essentially the same as Run F except that the hydrophilic polymer solution is not used and in its place is used a cycle of nitrogen-water slugs.
- Tests were conducted in a linear Benoist Sandstone core having 20.4 percent porosity and permeability of 176 millidarcies. The data are given In Table V below.
- gas injected into the formation is selected from the group consisting of air, nitrogen, carbon dioxide, flue gas, engine exhaust gas, methane, ethane, propane, butane, ethylene, propylene, butylene, natural gas, liquefied petroleum gas, and mixtures thereof.
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Abstract
The oil recovery efficiency of a tertiary oil recovery process such as a surfactant flood is improved by injecting after the surfactant solution alternating cycles of water and small volume slugs of a gas such as air, nitrogen, carbon dioxide, flue or exhaust gas, natural gas, methane, ethane, propane, butane, liquefied petroleum gas and mixtures thereof.
Description
IPTzilZ United States Patent 1191 Carlin May 13, 1975 [541 TERTIARY OIL RECOVERY PROCESS 3,529,668 9/1970 Bernard 166/273 INVOLVING MULTIPLE CYCLES 0F GAS'WATER INJECTION AFTER 3:599:7l6 8/1971 Thompson 166/273 SURFACTAN FLOOD 3,599,717 8/1971 McMillen 166/273 3,648,772 3/1972 Earlougher, Jr..... 166/273 [75] Inventor Joseph Caflm Houston 3,653,440 4/1972 Reisberg 166/273 [73] Assignee: Texaco Inc., New York, NY.
Primary ExaminerStephen J. Novosad [22] Flled' Dec. 1973 Attorney, Agent, or Firm-T. H. Whaley; C. G. Ries; [21] Appl. No.: 425,593 Jack H. Park 521 U.S. c1 166/273;' 166/274 [57] ABSTRACT [51] Int. Cl E21b 43/22 The Oil recovery efficiency of a tertiary Oil recovefy 58 Field of Search 166/273, 274, 270, 252 Process Such as a Surfactant flood is improved y jecting after the surfactant solution alternating cycles [56] References Cited of water and small volume slugs of a gas such as air, UNITED STATES PATENTS nitrogen, carbon dioxide, flue or exhaust gas, natural gas, methane, ethane, propane, butane, liquefied petroleum g and mixtures thereof.
3,472,320 10 1969 Dyes 166/273 9 Claims, 1 Drawing Figure JUAF/IC- W/Ufl? M/Vl' W/UZ'A MUZI/Plf GAP F1000 fl000 F2000 WATER //Vz/[[T/0/VJ m0 3 L) 4a PfiE'JJZ/RE E. w 0/FFE/FiA/7714Z 00 Z0 w 5 6 1 7 3 S g 70 0 5, a S 5 0/2 /?(0V/?V Q1 u E JU k 7 S 9 It N I N I 40 0/1 JAlZ/R/IT/O/V 17 -WAI'ER-0/L mr/a 3 :3
30 Q o m k LE 20 l l l l J l TERTIARY OIL RECOVERY PROCESS INVOLVING MULTIPLE CYCLES OF GAS-WATER INJECTION AFTER SURFACTANT FLOOD BACKGROUND OF THE INVENTION 1. Field of the Invention This invention pertains to an oil recovery process and more particularly to a process for tertiary oil recovery. Still more particularly this invention is concerned with a method of treating an oil containing formation after the formation has been subjected to chemical tertiary I oil recovery treatment such as surfactant flooding so as r permitting the petroleum to flow to the surface through these wells. Recovery of petroleum from petroleum containing formations is possible only if certain conditions are satisfied. There must be an adequately high concentration of petroleum in the formation, and there must be sufficient porosity and permeability or interconnected flow channel throughout the formation to permit the flow of fluids therethrough if sufficient pressure is applied to the fluid. When the subterranean petroleum containing formation has natural energy present in the form of an underlying active water drive, or gas dissolved in the petroleum, or a high pressure gas cap above the petroleum within the petroleum reservoir, this natural energy is utilized to recover petroleum. Recovery of petroleum by utilization of natural energy is referred to as primary recovery. When this natural energy source is depleted, or in the instance of those formations which do not originally contain sufficient natural energy to permit primary recovery operations, some form of supplemental recovery process must be utilized in order to extract petroleum from the subterranean petroleum containing formation. Supplemental recovery is frequently referred to as secondary recovery, although in fact it may be primary, secondary or tertiary in sequence of employment.
Water flooding, which involves the injection of water into the subterranean,petroliferous formation for the purpose of displacing petroleum toward the producing well, is the most economical and most widely practiced supplemental recovery method. Water does not displace petroleum with high efficiency, however, since water and oil are immiscible, and also because the interfacial tension between water and oil is quite high. Persons skilled in the art of oil recovery have recognized this weakness of waterflooding and many additives have been described in the prior art for decreasing the interfacial tension between the injected water and the formation petroleum. For example, U.S. Pat. No. 2,233,381 (1941) disclosed the use of polyglycol ether as a surface active agent or surfactant to increase the capillary displacement efficiency of an aqueous flooding medium. U.S. Pat. No. 3,302,713 discloses the use of petroleum sulfonate prepared from the 850 to l050F. boiling range fraction of petroleum crude as a surfactant for use in oil recovery operations. U.S. Pat.
'No. 3,468,377 (1969) describes the use of petroleum sulfonates of a specified molecular weight for oil recovery. Other surfactants which have been proposed for oil recovery include alkylpyridinium salts, alkyl sulfates, alkyl sulfonates, alkylaryl sulfonates and quaternary ammonium salts. Special surfactants or combinations of two or more dissimilar surfactants are sometimes required for use in formations having unusual properties such as formation water containing intolerably high concentrations of salt or polyvalent ions such as calcium or magnesium.
The cost of surfactants and other additives such as viscosity increasing polymers for drive fluids used in supplemental recovery is quite high, however, and the amount of additional oil recovered as a consequence of using surfactants has frequently not been sufficient to justify the use of chemical tertiary recovery on a commercial basis, even though there is a substantial need for the additional oil recoverable thereby.
In view of the foregoing, it can be appreciated that there is a substantial need for a method for increasing the volume of additional oil recovered by surfactant flooding without increasing the cost of the supplemental recovery process appreciably.
SUMMARY OF THE INVENTION This invention pertains to a novel process to be applied to a subterranean, petroleum containing formation which normally will already have been subjected to primary recovery and possibly waterflooding. The process is an additional step to be performed after subjecting the formation to chemical tertiary or supplemental oil recovery process such as flooding with a surfactant solution or a micellar dispersion. l have discovered that by injecting at least one and preferably several slugs of a gaseous substance into the formation after the chemical displacing fluid has been injected, substantial additional oil may be recovered. From 1 to 15 and preferably from 2 to 6 discrete slugs of gas, each gas slug being from 1/10 to 10 pore volume percent and preferably from 2 to 8 pore volume percent in size, with water slugs of from 10 to 50 pore volume percent interposed therebetween, are used after the chemical flood. Gaseous materials suitable for use in this process include air, nitrogen, carbon dioxide, flue gas, exhaust gas, methane, ethane, propane, butane, natural gas, liquefied petroleum gas (LPG) and mixtures thereofjMy invention, therefor, comprises the process of using small, alternating gas and water slugs after a chemical flood such as an aqueous surfactant containing fluid.
BRIEF DESCRIPTION OF THE DRAWING I The attached FIGURE illustrates the graphical results of a typical laboratory core displacement test, showing the pressure differential, percent oil recovery, residual oil saturation and water-oil ratio for a conventional waterflood followed by a surfactant flood followed by water injection followed by four cycles of gaswater injection.
DETAIL DESCRIPTION OF THE PREFERRED EMBODIMENTS Briefly, the process of my invention concerns an improvement in surfactant flooding. Surfactant flooding has been recognized by persons skilled in the art as a means for obtaining additional oil from an oil containing formation beyond that recoverable by primary recovery and waterflooding. For purposes of clarity, the following explanation of surfactants and surfactant flooding provides a basis for understanding the prior art process with which my invention is to be used.
The term surfactant encompasses a broad spectrum of materials which share the following common characteristics:
l. The compound must be at least slightly soluble in at least one phase of the liquid system in which it is to be used.
2. The compound must have an amphipathic structure (the molecule is composed of groups with opposing solubility tendencies). For use in oil recovery operations, the molecule must have at least one hydrophobic or oil soluble group and at least one hydrophilic or water soluble group.
3. Surfactant molecules or ions tend to form oriented monolayers at phase interfaces.
4. The equilibrium concentration of the surfactant in any particular solute is greater at the phase interface than the concentration of the surfactant in the bulk of the solution.
5. The materials tend to form micelles or aggregates of molecules or ions whenever the concentration exceeds a certain limiting value which is a characteristic of the particular surfactant and solute.
6. The material must exhibit some combination of the following functional properties: detergency, foaming, wetting, emulsifying, solubilizing and dispersing.
Surfactants are generally classified in the literature on the basis of the type of hydrophilic or water soluble group or groups attached to the molecule, generally being classified as anionic, cationic or nonionic, as described below more fully.
l. Anionic surfactants are those surfactant materials wherein the hydrophilic or water soluble group is a carboxylate, sulfonate, sulfate or phosphate group. This is the most important class of surfactants generally and as applied to oil recovery. Anionic surfactants are readily available, inexpensive, and have a high degree of surface activity. Petroleum recovery operations will generally involve the use of anionic surfactants unless there is some objection to the use of anionic surfactants, or some sufficient reason to resort to the use of some other compound. Petroleum sulfonates are currently very popular anionic surfactants for oil recovery, and are prepared by isolating a preselected boiling range fraction of a crude oil and subjecting it to sulfonation. Petroleum sulfonates are desirable for use in oil recovcry because of their effectiveness and low unit cost. Petroleum sulfonates do have certain limitations, however, notably their ineffectiveness in formations containing saline (high salt containing) or hard water (water having dissolved therein excessive quantities of polyvalent ions such as calcium and/or magnesium).
2. Cationic surfactants employ primary, secondary, or tertiary amines, or quaternary ammonium groups, as the hydrophilic or water soluble group.
3. Nonionic surfactants are materials which have no charge when the material is dissolved in an aqueous medium. The hydrophilic tendency is derived from oxygen atoms in the molecule which hydrate by hydrogen bonding to water molecules present in the solute. The strongest hydrophilic moiety in this class of surfactants is the ether linkage, and there must be a plurality of these linkages to render the compounds sufficiently water soluble to permit the compound to exhibit surface activity. Polyoxyethylene surfactants having the following recurring ether linkages are examples of hydrophilic moieties for nonionic surfactants:
A nonionic surfactant molecule may have more than one chain containing ether linkages and generally as much as 60 to percent by weight of the molecule must be in the form of ether linkage containing chains in order to render the molecule sufficiently water soluble for it to function as a surfactant. It can be readily seen that the presence of these large chains containing the ether linkages in addition to the relatively long aliphatic or other hydrophobic chains results in a high molecular weight compound. and this is one reason that nonionic surfactants have low surface activity per unit weight of material. Nonionic surfactants are seldom used alone in oil recovery applications, although they are frequently employed in combination with another surfactant material, generally an anionic material.
such as petroleum sulfonate or an alkylbenzene sulfonate, for the purpose of increasing the surfactants tolerance to salt or hard water.
Conventional practices today by persons skilled in the art of surfactant flooding involve the use of a multiplicity of steps only one of which may employ injecting a surfactant solution into the formation. The sequence may include injecting the following materials into the formation, generally in the order listed.
1. Usually water will have been injected to displace additional oil after primary recovery until the water-tooil ratio of the produced fluid becomes so high that further production is uneconomical.
2. A preflush may be used to remove or displace water soluble materials present in the formation water which interfere with the surfactant material to be used. Sacrificial compounds such as sodium carbonate, sodium polyphosphate, sodium fluoride, etc., may also be present in the preflush to saturate the adsorption sites of the formation rock so as to minimize adsorption thereon of the subsequently injected surfactant. This slug may be followed by an isolation slug of water.
3. The main displacing fluid is injected next, which may be an aqueous solution of one or several surfactants capable of reducing the interfacial tension between the formation petroleum and the injected aqueous fluids. The displacing fluid may also be an emulsion of a hydrocarbon in an aqueous surfactant solution.
4. A mobility buffer fluid is generally introduced into the formation subsequent to the surfactant solution to displace the solution efficiently. A small isolation slug of water is sometimes used between the surfactant solution and the mobility buffer fluid. The mobility buffer fluid is needed to ensure efficient displacement of surfactant solution and formation petroleum which has been displaced by the surfactant solution because the mobility of the petroleum is less than the mobility of water. Usually a dilute aqueous solution of a hydrophilic polymer such as polyacrylamide or a polysaccharide is used for this purpose. The concentration of polymer may be reduced gradually with time, or tapered, to essentially pure field water.
5. Water injection is continued until the water-oil ratio rises to an economically intolerable level.
By use of tertiary recovery programs such as are described above the percent oil recovery may often be increased by 10 to 20 percentage points, i.e., typically from 45 to 65 percent recovery, which may amount to millions of barrels of oil in a large field. Unfortunately the cost of the materials is frequently so great that such a program is not economically viable even though it is technically successful. a i
My discovery conce'rns an additional treatment step to be performed after completion of the surfactant'fluid injection step described above. The additional treatment involves the injection of a plurality of small discrete slugs of a gaseous material separated by injecting small slugs of liquid, preferably water or other aqueous fluids.
The volume of gas in each slug can be from 0.20 to 20 pore volume percent and usually the optimum size is from 2 to pore volume percent. The size of the water slug interposed between each gas slug injected can be from about 5 to about 50 pore volume percent, and preferably from about 10 to about pore volume percent. The number of discrete gas slugs injected can be from about 1 to about 20 and is preferably from about-2 to about 8 slugs.
Any material at least a portion of which will remain in the gaseous phase at the temperature and pressure of the formation may be used. Air, nitrogen, carbon dioxide, normally gaseous paraffinic hydrocarbons such as methane, ethane, propane or butane as well as normally gaseous olefinic hydrocarbons such as ethylene, propylene or butylene and mixtures thereof are preferred gases for use in my invention. Crude gases such as exhaust gas or flue gas, which are predominantly carbon dioxide and nitrogen, as well as natural gas or liquefied petroleum gas (LPG) may also be used with excellent results. Mixtures of any two or more of these materials may be used although care must be exercised if a mixture of air or other oxygen containing gas and a combustable gas are to be used.
Certain of the above gases are somewhat soluble in petroleum. For example, carbon dioxide and the paraffinic hydrocarbons such as methane, ethane, etc., or the olefinic gases are quite soluble to varying degrees in petroleum. This is beneficial to the operation of my process since dissolution of these gases results in reduction in the viscosity of the petroleum; however, the solubility must be taken into consideration when determining the gas slug size. By increasing the slug size so that more gas than will dissolve in petroleum is injected, at least a part of the injected petroleum soluble gases'will remain in the form of discrete, gaseous phase slugs in the formation. By this means, both the benefit of the process of my invention and of petroleum viscosity reduction by gas dissolution therein can be achieved simultaneously.
Gas injection has been described in the literature for petroleum recovery; however, it is recognized by persons skilled in the art that gas displaces petroleum in a very inefficient manner because the viscosity of gas is very much less than the viscosity of petroleum. The process of my invention differs considerably from gas displacement as taught by the prior art.
The mechanism responsible for the benefit resulting in employment is not fully understood. It is likely that the alternating gas-water slugs generate substantial mixing action in the formation, which aids in emulsification of oil or otherwise causes additional oil to move into the moving fluid stream. Also, gas appears to desorb surfactant from formation rock to a degree, making more surfactant available for oil displacement. The tendency of multiple gas slugs to desorb adsorbed surfactant from the formation matrix makes possible the use of substantially lower surfactant concentrations and/or smaller slugs of surfactant solutions in certain situations. It is not my intention to represent that these are necessarily the only mechanisms responsible for the benefits resulting from application of my invention, however.
In a slightly different embodiment of the process of my invention, the gas and water may be injected simultaneously after completion of injection of the surfactant solution into the formation. The volume ratio of gas and water being injected should be from about 0.002 to about 1.5 and preferably from about 0.5 to about 1.0. Some precaution should be taken to avoid excess vertical stratification of the gas and water, gas going exclusively into the top portion of the formation and water moving exclusively into the bottom portion, because of the large differences in density between water and gas. Such density related vertical separation can be prevented, for example, by providing two separate injection strings and injecting gas into the bottom of the formation and water into the top of the formation. This arrangement also permits separate control of the injection rate of each material to maintain the desired ratio of gas and water.
FIELD EXAMPLE In order to better understand the method of applying the process of my invention, the following pilotfield example is provided. This is merely one illustrative embodiment of my invention, however, and it is not intended to be limitative or restrictive thereof.
A subterranean, petroleum containing formation is found at a depth of 8000 feet. The formation is 40 feet thick and the porosity is 30 percent. The field is exploited first by primary production, utilizing a square grid pattern with 400 foot linespacing between wells. At the conclusion of primary recovery, which recovers only 25 percent of the original petroleum in place within the reservoir, injection wells are drilled in the center of each square grid to convert the field to an inverted five spot pattern for water injection. Although a large field entails a multiplicity of the square grid patterns, each 400 feet on a side and with an injection well in the center, it is possible to analyze the entire field by considering only a single grid unit. Water is injected into the injection well and production of oil is continued from the production wells until the water/oil ratio reaches 30, which is considered to be the economic limit for continued production. At the conclusion of the water flooding operation, only 45 percent of the original oil in place in the reservoir has been recovered and the average residual oil saturation is 33 percent. Some form of tertiary recovery operation must be employed in order to obtain any significant portion of the remaining petroleum. The formation water contains about 300 parts per million total hardness and low salinity, and tests indicate that petroleum sulfonate will function effectively therein. A tertiary chemical supplemental recovery program is designed using a 10 pore volume percent preflush comprising a 5 percent aqueous solution of sodium carbonate as a sacrificial adsorption agent followed by a 3 pore volume percent water slug to act as an isolation slug between the preflush and the surfactant slug. A 10 pore volume percent slug of 3.5 percent petroleum sulfonate is used as the surfactant slug. Since the pattern used results in percent sweep efficiency, the total pore volume swept by injected fluids in each grid segment is: 400 Ft. X 400 Ft.
EXPERIMENTAL In order to demonstrate the operability of my invention and to determine the optimum values for control parameters for the process of my invention, as well as 'to ascertain the magnitude of additional oil recovery resulting from employment thereof, the following experimental laboratory work was done.
' A linear core taken from the Slaughter Field, Hockley County, Texas was evaluated for chemical tertiary recovery. Because the formation water is high in calcium and magnesium content, a special surfactant combination consisting of a linear alkylbenzene sulfonate anionic surfactant and a polyethoxylated nonlyphenol nonionic surfactant was determined to be the optimum surfactant for use. The results of Run A, a core displacement test, is graphically illustrated in the attached figure, showing percent oil recovery, residual oil recovery, water-oil ratio of the produced fluid, and the differential pressure across the core, all as a function of the pore volumes of fluid injected into the core. As can be seen, a waterflood using 2.5 pore volumes of a mixture of 20 percent Slaughter Formation Connate Water followed by a surfactant flood using 1 pore volume of 0.4 percent linear alkylbenzene sulfonate and 0.4 percent of the nonionic surfactant followed by 2 pore volumes of water followed by four cycles of alternating gas water injection, 20 pore volume percent gas, air being used as the gas, and from 20 to 50 pore volumes percent of water for the water slugs between air slugs resulted in a total oil recovery of 87 percent and a residual oil saturation of about 9 percent. The significant end point values are tabulated in Table I below.
It can be seen that the total oil recovery was increased from 74 to 87.5 percent, anet increase of 18.2 percent in oil recovery as a result of the gas-water injection after completion of the chemical flood.
In order to compare the effect of continuing water injection after chemical flood to a high water-oil ratio the following pair of experiments were performed on a core taken from the Aux Vases formation, Salem Field, Marion County, Illinois. After waterflooding to a water-oil ratio of :1, two tertiary, displacements were performed. In Run B, a surfactant slug of 0.4 percent linear alkylbenzene sulfonate and 0.4 percent polyethoxylated alkylphenol was injected and then water was injected continually until the water-oil ratio was quite high, followed by a slug of gas and water. lnRun C, the same procedure was used except the step of Waterflooding to a high water-oil ratio after chemical flooding was omitted. The results are given in Table 11 below.
Several important observations may be made from the above data. Continuation of water injection after chemical flood to a very high water-oil ratio value was somewhat ineffective. Injection of gas-water slugs soon after completion of the chemical flood is much more effective than continuing waterflooding to a high water-oil ratio. Also, even if waterflooding to a high water-oil ratio is utilized, considerable additional oil can be recovered by initiating gas-water injection after the Waterflood.
In Run D, a core was subjected to a commercial waterflood employing a preflush with salinity optimization and containing sacrificial adsorption agents followed by an aqueous solution of petroleum sulfonate followed by an aqueous solution of a hydrophilic polymer for mobility control followed by waterflooding to a high water-oil ratio. A slug of nitrogen was then introduced and the core was again waterflooded.
It can be seen from the foregoing that considerable oil can be recovered after use of petroleum sulfonate and a polymer solution by a gas slug injection.
' 9 Instill another Salem co're' displacementexperiment, Run E was'performed as before exceptusing'two different commerciallyavailable surfactants-Ihesurfactant solution contained 1.0 percent Triton, a dioctyl sodium succinate and 0.25 percent TD-l5, a polyoxyalkalene ether. The results of Run E are given in Table IV below.
It can be seen that in Run E, the gas water slug had a more pronounced effect on oil recovery than did the chemical flood.
Two additional runs were made to compare a commercial chemical tertiary flood, Run F, comprising sacrificial agent preflush, petroleum sulfonate, hydrophilic polymer and waterflood to a high water-oil ratio, to a Run G which is essentially the same as Run F except that the hydrophilic polymer solution is not used and in its place is used a cycle of nitrogen-water slugs. Tests were conducted in a linear Benoist Sandstone core having 20.4 percent porosity and permeability of 176 millidarcies. The data are given In Table V below.
It can be seen that the surfactant-gas-water injection recovered 85.5 percent of the original oil compared to 74 percent for the conventional surfactant polymer flood, which amounts to a 15.5 percent improvement thereover.
Thus I have disclosed and demonstrated that by the use of at least one and preferably a plurality of small slugs of gas separated by water slugs, injected after a surfactant containing solution has been injected into a formation, the final oil recovery is increased materially, the residual oil saturation is reduced correspondingly, the amount of surfactant required is reduced, and the need for a solution of hydrophilic polymer containing, mobility buffer solution can at least in some instances be eliminated. While several explanations have been offered for the mechanisms responsible for the benefits resulting from the practice of my invention, I do not intend that I be bound thereby and I do not hereby represent that these are the only or even the major mechanisms responsible for the benefits attained by the practice of the process of my invention. Similarly, while several illustrative embodiments have been disclosed herein, my invention is not so limited, as many more i 10 variations thereover will be apparent to persons skilled in the'related arts without departing from the true spirit I and scope of my invention, and therefore it is my intention that my invention be limited and restricted only by those limitations and restrictions which are contained in the claims appended hereinafter.
I claim:
1. In a method for recovering petroleum from a subterranean, petroleum containing, porous formation penetrated by at least one injection well and at least one production well, both wells being in fluid communication with the formation, said recovery method being of the type wherein an aqueous surfactant solution is injected into the formation and an aqueous solution of hydrophilic, viscosity increasing polymer is injected into the formation following the surfactant solution and oil displaced by the injected fluids is recovered from the formation via the production well, wherein the improvement comprises:
a. injecting from about 2 to about 8 slugs of gas the volume of which is from about 0.2 to about 20.0 pore volume percent with a slug of from about 5 to about 50 pore volume percent water injected between succeeding gas slugs into the formation after injection of the solution of the hydrophilic viscosity increasing polymer; and
b. injecting water into the formation after injection of all of the slugs of gas to displace the gas, surfactant solution and solution of hydrophilic viscosity increasing buffer and formation petroleum toward the production well.
2. A method as recited in claim 1 wherein the gas injected into the formation is selected from the group consisting of air, nitrogen, carbon dioxide, flue gas, engine exhaust gas, methane, ethane, propane, butane, ethylene, propylene, butylene, natural gas, liquefied petroleum gas, and mixtures thereof.
3. A method as recited in claim 2 wherein the gas is air.
4. A method as recited in claim 2 wherein the gas is nitrogen.
5. A method as recited in claim 2 wherein the gas is carbon dioxide.
6. A method as recited in claim 2 wherein the gas is methane.
7. A method as recited in claim 2 wherein the gas is natural gas.
8. A method as recited in claim 2 wherein the gas is liquefied petroleum gas. I
9. In a method of recovering petroleum from a sub terranean, porous, petroleum containing formation penetrated by at least one injection well having at least two separate injection paths from the surface of the earth to the petroleum containing formation, one being in fluid communication with the upper portion of the formation and one being in fluid communication with the lower portion of the formation, and at least one production well, said recovery method being of the type wherein a surfactant containing recovery fluid is injected into the formation via the injection well and fluids including formation petroleum are recovered from the production well, the improvement which comprises:
simultaneously injecting into the formation, gas via the injection path in fluid communication with the lower portion of the formation and water via the injection path in fluid communication with the 12 dioxide, flue gas, exhaust gas, methane, ethane, propane, butane, ethylene, propylene, butylene, natural gas, liquefied petroleum gas, and mixtures thereof.
Claims (9)
1. IN A METHOD FOR RECOVERING PETROLEUM FROM A SUBTERRANEAN, PETROLEUM CONTAINING PORUS FORMATION PENETRATED BY AT LEAST ONE INJECTION WELL AND AT LEAST ONE PRODUCTION WELL, BOTH WELLS BEING IN FLUID COMMUNICATION WITH THE FORMATION SAID RECOVERY METHOD BEING OF THE TYPE WHEREIN AN AQUEOUS SURFACTANT SOLUTION IS INJECTED INTO THE FORMATION AND AN AQUEOUS SOLUTION OF HYDROPHILICC, VISOCITY INCREASING POLYMER IS INJECTED INTO THE FORMATION FOLLOWING THE SURFACTAT SOLUTION AND OIL DISPLACED BY THE INJECTED FLUIDS IS RECOVERED FROM THE FORMATION VIA THE PRODUCTION WELL, WHEREIN THE IMPROVEMENT COMPRISES: A. INJECTING FROM ABOUT 2 TO ABOUT 8 SLUGS OF GAS THE VOLUME OF WHICH IS FROM ABOUT 0.2 TO ABOUT 20.0 PORE VOLUME PERCENT WITH A SLUG OF FROM ABOUT 5 TO ABOUT 50 PORE VOLUME PERCENT WATER INJECTED BETWEEN SUCCEEDING GAS SLUGS INTO THE FORMATION AFTER INJECTION OF THE SOLUTION OF THE HYDROPHILIC VISCOSITY INCREASING POLYMER; AND B. INJECTING WATER INTO THE FORMATION AFTER INJECTION OF ALL OF THE SLUGS OF GAS TO DISPLACE THE GAS, SURFACTANT SOLUTION AND SOLUTION OF HYDROPHILIC VISCOSITY INCREASING BUFFER AND FORMATION PETROLEUM TOWARD THE PRODUCTION WELL.
2. A method as recited in claim 1 wherein the gas injected into the formation is selected from the group consisting of air, nitrogen, carbon dioxide, flue gas, engine exhaust gas, methane, ethane, propane, butane, ethylene, propylene, butylene, natural gas, liquefied petroleum gas, and mixtures thereof.
3. A method as recited in claim 2 wherein the gas is air.
4. A method as recited in claim 2 wherein the gas is nitrogen.
5. A method as recited in claim 2 wherein the gas is carbon dioxide.
6. A method as recited in claim 2 wherein the gas is methane.
7. A method as recited in claim 2 wherein the gas is natural gas.
8. A method as recited in claim 2 wherein the gas is liquefied petroleum gas.
9. In a method of recovering petroleum from a subterranean, porous, petroleum containing formation penetrated by at least one injection well having at least two separate injection paths from the surface of the earth to the petroleum containing formation, one being in fluid communication with the upper portion of the formation and one being in fluid communication with the lower portion of the formation, and at least one production well, said recovery method being of the type wherein a surfactant containing recovery fluid is injected into the formation via the injection well and fluids including formation petroleum are recovered from the production well, the improvement which comprises: simultaneously injecting into the formation, gas via the injection path in fluid communication with the lower portion of the formation and water via the injection path in fluid communication with the upper portion of the formation, both the gas and water being injected after injection of the surfactant containing fluid is completed, the ratio of gas volume flow rate to water flow rate being from about 0.002 to about 1.5, said gas being selected from the group consisting of air, nitrogen, carbon dioxide, flue gas, exhaust gas, methane, ethane, propane, butane, ethylene, propylene, butylene, natural gas, liquefied petroleum gas, and mixtures thereof.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US425593A US3882940A (en) | 1973-12-17 | 1973-12-17 | Tertiary oil recovery process involving multiple cycles of gas-water injection after surfactant flood |
| DE2443070A DE2443070A1 (en) | 1973-12-17 | 1974-09-09 | PROCESS FOR OIL RECOVERY FROM AN UNDERGROUND POROUS FORMATION |
| CA209,433A CA1001549A (en) | 1973-12-17 | 1974-09-17 | Tertiary oil recovery process involving multiple cycles of gas-water injection after surfactant flood |
| GB4304374A GB1471567A (en) | 1973-12-17 | 1974-10-04 | Tertiary oil recovery process involfing multiple cycles of gas-water injection after surfactant flood |
| AU74370/74A AU7437074A (en) | 1973-12-17 | 1974-10-16 | Oil recovery process |
| BR10404/74A BR7410404D0 (en) | 1973-12-17 | 1974-12-12 | PROCESS FOR PETROLEUM RECOVERY FROM AN UNDERGROUND POROUS FORMATION CONTAINING PETROLEUM |
| NO744505A NO744505L (en) | 1973-12-17 | 1974-12-13 | |
| AR256945A AR216041A1 (en) | 1973-12-17 | 1974-12-17 | METHOD TO RECOVER OIL FROM AN UNDERGROUND POROUS PETROLEUM FORMATION |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US425593A US3882940A (en) | 1973-12-17 | 1973-12-17 | Tertiary oil recovery process involving multiple cycles of gas-water injection after surfactant flood |
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| US3882940A true US3882940A (en) | 1975-05-13 |
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|---|---|---|---|
| US425593A Expired - Lifetime US3882940A (en) | 1973-12-17 | 1973-12-17 | Tertiary oil recovery process involving multiple cycles of gas-water injection after surfactant flood |
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| Country | Link |
|---|---|
| US (1) | US3882940A (en) |
| AR (1) | AR216041A1 (en) |
| AU (1) | AU7437074A (en) |
| BR (1) | BR7410404D0 (en) |
| CA (1) | CA1001549A (en) |
| DE (1) | DE2443070A1 (en) |
| GB (1) | GB1471567A (en) |
| NO (1) | NO744505L (en) |
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| US4034810A (en) * | 1975-12-01 | 1977-07-12 | Phillips Petroleum Company | Oil recovery |
| US4415032A (en) * | 1982-04-27 | 1983-11-15 | Mobil Oil Corporation | Carbonated waterflooding for viscous oil recovery using a CO2 solubility promoter and demoter |
| US4544206A (en) * | 1982-12-13 | 1985-10-01 | Phillips Petroleum Company | Slug-type in situ recovery of mineral values |
| US4609478A (en) * | 1984-02-21 | 1986-09-02 | Olin Corporation | Sulfonated alkyl glucosides and use thereof in oil recovery |
| US4846276A (en) * | 1988-09-02 | 1989-07-11 | Marathon Oil Company | Water-alternating-gas flooding of a hydrocarbon-bearing formation |
| US5046560A (en) * | 1988-06-10 | 1991-09-10 | Exxon Production Research Company | Oil recovery process using arkyl aryl polyalkoxyol sulfonate surfactants as mobility control agents |
| US5267615A (en) * | 1992-05-29 | 1993-12-07 | Christiansen Richard L | Sequential fluid injection process for oil recovery from a gas cap |
| US5363914A (en) * | 1993-03-25 | 1994-11-15 | Exxon Production Research Company | Injection procedure for gas mobility control agents |
| WO1995027839A1 (en) * | 1994-04-11 | 1995-10-19 | Marathon Oil Company | Enhanced oil recovery from heterogeneous reservoirs |
| US6186231B1 (en) | 1998-11-20 | 2001-02-13 | Texaco Inc. | Conformance improvement in hydrocarbon bearing underground strata using lignosulfonate-acrylic acid graft copolymer gels |
| US6942031B1 (en) * | 1995-11-27 | 2005-09-13 | Texaco Inc. | Lignosulfonate-acrylic acid graft copolymers as sacrificial agents for carbon dioxide foaming agents |
| RU2266396C2 (en) * | 2003-09-12 | 2005-12-20 | Савицкий Николай Владимирович | Method and device for oil pool development |
| US20060180306A1 (en) * | 2003-05-12 | 2006-08-17 | Stone Herbert L | Method for improved vertical sweep of oil reservervoirs |
| RU2290500C1 (en) * | 2005-06-23 | 2006-12-27 | ОАО "Татнефть" им. В.Д. Шашина | Method for inter-well transit of liquid |
| RU2339799C1 (en) * | 2007-02-13 | 2008-11-27 | Закрытое акционерное общество ПАРМ-ГИНС | Method for development of massive oil deposit |
| US20130087072A1 (en) * | 2005-11-15 | 2013-04-11 | Queen's University At Kingston | Reversibly Switchable Surfactants and Methods of Use Thereof |
| US20130200291A1 (en) * | 2012-01-27 | 2013-08-08 | Queen's University At Kingston | Tertiary Amine-Based Switchable Cationic Surfactants and Methods and Systems of Use Thereof |
| US10377647B2 (en) | 2010-12-15 | 2019-08-13 | Queen's University at Kingson | Systems and methods for use of water with switchable ionic strength |
| CN112343567A (en) * | 2020-10-20 | 2021-02-09 | 中国石油化工股份有限公司 | Chemical flooding injection method based on high-water-content oil reservoir with large water channel |
| US11498853B2 (en) | 2010-02-10 | 2022-11-15 | Queen's University At Kingston | Water with switchable ionic strength |
| CN119933583A (en) * | 2023-11-01 | 2025-05-06 | 中国石油天然气股份有限公司 | A method for adjusting plugging and driving of a horizontal well fixed pipe string |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2123105C1 (en) * | 1997-06-16 | 1998-12-10 | Закрытое акционерное общество "Интойл" | Method of developing oil pool |
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| US3386506A (en) * | 1966-04-08 | 1968-06-04 | Pan American Petroleum Corp | Method for secondary recovery of petroleum |
| US3472320A (en) * | 1965-01-27 | 1969-10-14 | Alvin B Dyes | Secondary recovery method using alternate slugs of gas and water |
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- 1974-09-17 CA CA209,433A patent/CA1001549A/en not_active Expired
- 1974-10-04 GB GB4304374A patent/GB1471567A/en not_active Expired
- 1974-10-16 AU AU74370/74A patent/AU7437074A/en not_active Expired
- 1974-12-12 BR BR10404/74A patent/BR7410404D0/en unknown
- 1974-12-13 NO NO744505A patent/NO744505L/no unknown
- 1974-12-17 AR AR256945A patent/AR216041A1/en active
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| US3244228A (en) * | 1962-12-27 | 1966-04-05 | Pan American Petroleum Corp | Flooding process for recovery of oil |
| US3472320A (en) * | 1965-01-27 | 1969-10-14 | Alvin B Dyes | Secondary recovery method using alternate slugs of gas and water |
| US3386506A (en) * | 1966-04-08 | 1968-06-04 | Pan American Petroleum Corp | Method for secondary recovery of petroleum |
| US3529668A (en) * | 1968-07-24 | 1970-09-22 | Union Oil Co | Foam drive oil recovery process |
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Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4034810A (en) * | 1975-12-01 | 1977-07-12 | Phillips Petroleum Company | Oil recovery |
| US4415032A (en) * | 1982-04-27 | 1983-11-15 | Mobil Oil Corporation | Carbonated waterflooding for viscous oil recovery using a CO2 solubility promoter and demoter |
| US4544206A (en) * | 1982-12-13 | 1985-10-01 | Phillips Petroleum Company | Slug-type in situ recovery of mineral values |
| US4609478A (en) * | 1984-02-21 | 1986-09-02 | Olin Corporation | Sulfonated alkyl glucosides and use thereof in oil recovery |
| US5046560A (en) * | 1988-06-10 | 1991-09-10 | Exxon Production Research Company | Oil recovery process using arkyl aryl polyalkoxyol sulfonate surfactants as mobility control agents |
| US4846276A (en) * | 1988-09-02 | 1989-07-11 | Marathon Oil Company | Water-alternating-gas flooding of a hydrocarbon-bearing formation |
| US5267615A (en) * | 1992-05-29 | 1993-12-07 | Christiansen Richard L | Sequential fluid injection process for oil recovery from a gas cap |
| US5363914A (en) * | 1993-03-25 | 1994-11-15 | Exxon Production Research Company | Injection procedure for gas mobility control agents |
| WO1995027839A1 (en) * | 1994-04-11 | 1995-10-19 | Marathon Oil Company | Enhanced oil recovery from heterogeneous reservoirs |
| US5465790A (en) * | 1994-04-11 | 1995-11-14 | Marathon Oil Company | Enhanced oil recovery from heterogeneous reservoirs |
| US6942031B1 (en) * | 1995-11-27 | 2005-09-13 | Texaco Inc. | Lignosulfonate-acrylic acid graft copolymers as sacrificial agents for carbon dioxide foaming agents |
| US6186231B1 (en) | 1998-11-20 | 2001-02-13 | Texaco Inc. | Conformance improvement in hydrocarbon bearing underground strata using lignosulfonate-acrylic acid graft copolymer gels |
| US20060180306A1 (en) * | 2003-05-12 | 2006-08-17 | Stone Herbert L | Method for improved vertical sweep of oil reservervoirs |
| US7303006B2 (en) * | 2003-05-12 | 2007-12-04 | Stone Herbert L | Method for improved vertical sweep of oil reservoirs |
| RU2266396C2 (en) * | 2003-09-12 | 2005-12-20 | Савицкий Николай Владимирович | Method and device for oil pool development |
| RU2290500C1 (en) * | 2005-06-23 | 2006-12-27 | ОАО "Татнефть" им. В.Д. Шашина | Method for inter-well transit of liquid |
| US20130087072A1 (en) * | 2005-11-15 | 2013-04-11 | Queen's University At Kingston | Reversibly Switchable Surfactants and Methods of Use Thereof |
| RU2339799C1 (en) * | 2007-02-13 | 2008-11-27 | Закрытое акционерное общество ПАРМ-ГИНС | Method for development of massive oil deposit |
| US11498853B2 (en) | 2010-02-10 | 2022-11-15 | Queen's University At Kingston | Water with switchable ionic strength |
| US10377647B2 (en) | 2010-12-15 | 2019-08-13 | Queen's University at Kingson | Systems and methods for use of water with switchable ionic strength |
| US20130200291A1 (en) * | 2012-01-27 | 2013-08-08 | Queen's University At Kingston | Tertiary Amine-Based Switchable Cationic Surfactants and Methods and Systems of Use Thereof |
| CN112343567A (en) * | 2020-10-20 | 2021-02-09 | 中国石油化工股份有限公司 | Chemical flooding injection method based on high-water-content oil reservoir with large water channel |
| CN119933583A (en) * | 2023-11-01 | 2025-05-06 | 中国石油天然气股份有限公司 | A method for adjusting plugging and driving of a horizontal well fixed pipe string |
Also Published As
| Publication number | Publication date |
|---|---|
| NO744505L (en) | 1975-07-14 |
| CA1001549A (en) | 1976-12-14 |
| GB1471567A (en) | 1977-04-27 |
| BR7410404D0 (en) | 1975-09-16 |
| AU7437074A (en) | 1976-04-29 |
| DE2443070A1 (en) | 1975-07-03 |
| AR216041A1 (en) | 1979-11-30 |
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